Barely Significant
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Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disorders.

J Med Genet · 2022 · PMC8273188 · PMID 33436522

Europe PMCDOI
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hedged sentence
0.0000
closest p · 0.0× alpha
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boldest claim

The sentences

highly significantp=0.00003actually significant
Compared with population data, enrichment of SIX1 loss-of-function variants was highly significant (p=0.00003).

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